E&P Tank Emissions Model User's Manual

Production Tank Emissions Model,
E&P TANK Version 3.0
Users Manual
API PUBLICATION 4697
Chapter 1: Introduction
Welcome
Welcome to E&P TANK Version 3.0, a software program that predicts hydrocarbon
emissions from production oil tanks. This version of E&P TANK is compatible with both 32bit and 64-bit Windows 7 as well as Windows 2000/XP/Vista.
Whats New in This Version

The new capabilities and functions of E&P TANK v3.0 include:
1. Plus Fraction Characterization Algorithm
A flexible plus fraction (Cn+) characterization algorithm has been implemented in this
version. Users have the option of inputting inlet streams containing C7+, C8+, C9+, or C10+
component groups depending on the data availability from the lab analysis. The fluid is
characterized by employing an exponential distribution function to estimate the composition
profile of the heaviest components and a re-grouping and averaging process to generate the
critical properties for five (5) pseudo-components to represent the plus fraction with carbon
number greater than 7.
2. Updated with the Stream Input Algorithm
Modifications have been made on the existing four (4) options of the stream input.
Low Pressure Oil This option is used as direct input for emission calculations. In
this case, the low pressure oil from the separator is passed through a flash valve in
which the pressure is reduced. The flash loss is estimated based on the conditions of
the separator as well as the ambient temperature and pressure. A pressure-enthalpy
(P-H) flash calculation is used to take into account the pressure drop. In addition, the
separator temperature and pressure are also required for the calculation of the
specific gravity of flash oil. The characterization of Cn+ fraction as described above is
performed prior to the flash calculation.
High Pressure Oil This option has been updated. An initial calculation is performed
to estimate the composition of low pressure oil. The estimated composition of the low
pressure oil is used in the algorithm for low pressure oil input as described above to
calculate the flash loss and the specific gravity of flash oil.
Low Pressure Gas This option has been revised. Molar ratios (C7:C8:C9:C10) are no
longer required as inputs. Instead, the gas-oil ratio (GOR) is a required input to
PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL
generate the composition of high pressure oil through iterative calculations. Once the
high pressure oil composition is obtained, the program uses the procedures
described in the High Pressure Oil section are used to estimate the flash losses and
specific gravity of the flash oil.
Geographic Database This option is used in the cases where lab analysis is not
available. The existing database remains unchanged from v2.0 and contains 103
cases divided into four geographic regions and classified by sales oil properties (API
and RVP) and separator conditions (temperature and pressure).
3. Mass Balance and Green House Gas Emission Calculations

A mass balance routine is used to calculate and display the emission results for the flash
gas loss, the W/S gas losses, and total emission. The report also displays the uncontrolled
emissions of CO2 and CH4 separately in addition to total HAPs, total HC, and VOCs (both
controlled and uncontrolled).
4. Monthly Reports
An option has been added to display the results of emission calculations for the production
tanks on a monthly basis to reflect differences in ambient and tank operating conditions from
month to month during the year. Input stream composition and separator conditions are
assumed to be constant and cannot be varied on a monthly basis.
Both the RVP Distillation Column model and the AP-42 model can be used to perform
monthly calculations. If the RVP Distillation Column model is chosen, the required monthly
inputs are ambient temperatures, ambient pressures, and average daily production rates for
sales oil. If the AP-42 model is chosen, the additional inputs required include the monthly
average highest and lowest ambient daily temperatures and the solar insolation factor for
each month based on meteorological data. The emission results based on the selected
months as well as the total emission for the selected time period are displayed in a table
format and can be exported to an Excel file or a text file and plotted for comparison.
5. Modifications to the Graphical User Interface (GUI)
The GUI has been significantly improved to include the new functions and calculation
routines. Specifically, the major improvements include:
Compatibility with 32-bit and 64-bit Windows 7, and Windows XP operating systems.
Measurement unit system options The user may select either English or SI units or
create his/her own unit system by mixing the two unit systems (for example, bar for
pressure and C for temperature).
A choice of either monthly or yearly report display options.
The ability to export input / output results to MS Excel spreadsheet.
6. Compatibility between Version 2.0 and Version 3.0

The program v3.0 can open a case created by v2.0 and re-save it as v3.0 case which will be
indicated as .ept3 as compared to .ept in v2.0. However, cases saved in v3.0 (.ept3) cannot
be opened or processed by v2.0 software.
About E&P TANK Version 3.0

Petroleum production tank batteries are prevalent within the petroleum industrys exploration
and production (E&P) sector. Tank operators are required to quantify and report certain tank
emissions. These may include both Hazardous Air Pollutants (HAPs) and Volatile Organic
Compounds (VOCs). The following table shows the types of HAPs and VOCs considered in
this program.
HAPs
VOCs
Benzene
Methane
Octanes
Toluene
Ethane
Nonanes
Ethyl-Benzene
Propane
Benzene
Xylenes
n-Butane
Toluene
n-Hexane
i-Butane
Ethyl-Benzene
n-Pentane
Xylenes
i-Pentane
Heptanes+
n-Hexane
Octanes+
Hexanes
Nonanes+
Heptanes
Decanes+
A study previously undertaken by the API evaluated alternatives for quantifying the
hydrocarbon emissions from petroleum production tanks [1]. The study concluded that direct
field sampling and analysis from each production tank were deemed not feasible from
economic and technical viewpoints. Therefore, development of a computer-based simulator
for estimating emissions was recommended.
The calculation algorithm of this software follows the recommendation of a previous API
study [1]. A steady-state model is used to simulate petroleum production tank operations.
The contribution by flash losses to the total vent from the tanks is calculated rigorously
according to thermodynamic principles. The working and standing losses are simulated
differently depending upon the nature of the tank. For oil production tanks, the working and
standing losses are represented by a distillation column operation, either of which will
generate a certain amount of vaporization so that the characteristics of the produced liquid
matches the sales oil specifications such as Reid Vapor Pressure (RVP). In addition, a
modified AP-42 method may be used instead of the distillation column method for calculating
working and standing losses from oil production tanks. For storage tanks containing stable
oil or sales oil, the work and standing losses are calculated by a modified AP-42 method.
Chapter 2: Installation and Security Methods

System Requirements
Standalone PC Edition
70 MB free hard disk space
Printer (optional)
Microsoft Windows 7/XP/2000/Vista
Microsoft Excel (for option to export)
Network Edition
Microsoft Network TCP/IP
Installing E&P TANK v3.0

1. Find the .msi file and double click it to start the installation
2. Change the default E&P TANK directory if desired
After installation, the E&P TANK program group will be created. The default installation directory
is: C:\Program Files\API\ EP Tank 3.0.
For further details please refer to the document EP_TanksV3_Installtion_Guide.pdf. Which is
can be downloaded by clicking the link.
Note: If there is already a version (including demos) of E&P TANK on your system, please
uninstall the existing version first. For further information on uninstalling, refer to your Microsoft
Windows Help system. Please ensure the regional language settings are English (US or
Canada) otherwise some features will not be accessible.
Chapter 3: Getting Started

Starting and Exiting E&P TANK Version 3.0
To Start E&P TANK v3.0
1.
Select E&P TANK from Program in the Start menu of the Windows Taskbar,
-orDouble-click EPTANK.exe file in the installation folder through Windows Explorer.
An introductory screen followed by the welcome window appears.
Welcome to the E&P TANK Program
2. In the Welcome to the E&P TANK Program dialog, select appropriate option to open a
new project, the last project, or an existing project and click OK.
Note: The security method must be properly configured to run E&P Tank. To see how to setup
security method, please refer to Chapter 2.
To Exit E&P TANK v3.0

Do one of the following:
Click Exit from the File menu.
Click on the Close Box on the E&P TANK title bar.
Right click on the E&P TANK title bar and select Close.
Basic Steps to Generate an E&P TANK Project

The basic steps to create a project using E&P TANK v3.0:
1. Open a new project.
2. In the Project Setup window:
Select a flowsheet and a calculation model
Specify necessary setup information
Provide the project information if available
3. In the Data Input window, provide inputs via hotspots (devices or flow lines) on the input
flowsheet.
4. Execute calculations.
5. View and print results.
6. Save the project.
Working Environment
The application window of E&P TANK v3.0 can be divided into two main areas:
Function Palette
Data Operating Area
Function
Palette
Data Operating Area
The E&P TANK Application Window
Located in the left pane, the Function Palette consists of navigating buttons. Upon clicking on a
navigating button, the Data Operating Area to the right of the Function Palette displays the
corresponding window. There are three operating windows in E&P TANK:
Project Setup
Data Input
Data Output
The Data Operating Area occupies the right pane of the application window. It displays the
corresponding worksheet that you select from the Button Palette. The Data Operating Area is
the main working area where you can input data and view calculation results.
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Default Unit System Selection

The Default Unit System Selection allows the option to work with the English units, the SI Units
or the Customized Units.
Default Unit System Selection
Unit Manager
Select Unit Conversion on the primary menu and then Start Unit Manager. The Unit
Manager window is composed of three main sections:
The default unit system selection
The parameter tab
The parameter selection on the left corner
The parameter (Pressure, Volume, Temperature etc.) tab, displays the number of Unit Items,
customized units and also a data area where all the conversion parameter values are listed.
Conversion Parameters Tab

There are two unit systems available in E&P TANK: English and SI units. Users may choose to
view data and print projects in either of the units, regardless of which system was used in data
input. To select a unit system, click on the appropriate unit buttons on the toolbar or select from
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the Unit Conversion menu. Besides selecting the unit system, users may select mol % or wt %
from the toolbar or the Unit Conversion menu.
Unit Conversion
To perform unit conversions:
Select the unit to be converted from, by scrolling through the list of units in the from
field.
Select the unit to be converted to, by scrolling through the list of units in the To
window.
Input the Value to be converted in the white blank area.
Chapter 4: Using E&P TANK Version 3.0

Creating a New Project
When you are starting E&P TANK v3.0:
In the welcome window, select Create a New E&P TANK Project and click OK.
-orWhile you are working on another project, click on the New Project button on the toolbar or
select New from the File menu.
Project Setup
Project Setup
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To Setup a Project
1. On the Configuration tab in the Project Setup window:
a. Make a Flowsheet Selection
b. Select a model to calculate Working and Standing (W&S) losses. Regardless of which
model you select in step 2, E&P TANK uses the Peng-Robinson equation of state to
calculate flash loss.
c. If the flowsheet with separator was selected in Step 1a, select a Separator Stream for
which compositional information is known.
d. Click to select Control Efficiency and specify the percentage, if desired.
e. Select Calculation Basis. If Monthly is selected, specify which month(s) to calculate.
f.
Make a Component Group selection from the drop-down menu reflecting the last Cn+ in
the input stream analytical data.
g. If you select flowsheet with separator in Step 1a and RVP as calculation model in Step
1b, the Air Injection option will be available for you to specify the daily air injection.
2. Switch to the Project Description tab to enter details about the facility. This information will
help identify the project.
Note: Once a Cn+ group is selected and the characterization is completed, the component
group selection option will be dimmed and changes in the Cn+ group will not be allowed.
Data Input
The Data Input flowsheet is object oriented. The flowsheet changes according to your project
setup. Hotspots are colored green in the flowsheet.
Some but not all of the following inputs are required for each project:
Separator
Stable Oil Tank
Stable Oil and Sales Oil
Flash Valve Inputs
Air Injection
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Input Flowsheet: Tank with Separator
Separator
Users enter the input data such as separator conditions and detailed compositional data for
separator oil or gas. The input varies according to your selection of Known Separator Stream
Information in the Project Setup window.
Data Input for Low Pressure or High Pressure Oil

If Low Pressure Oil or High Pressure Oil is selected as the known separator stream in Project
Setup, an input dialog similar to the one shown in the following will appear when you click on the
Separator hotspot.
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To input data for the LP/HP Oils:

1. Click on the Separator hotspot on the Input Flowsheet. The input dialog appears.
Separator: High Pressure Oil Input
2. Provide Separator Conditions: Pressure and Temperature.

(Note: clicking on the triangular icon adjacent to the unit values allows the user to
modify the units for the associated inputs)
3. Enter the Composition of the low-pressure or high-pressure oil.
4. Provide the characterization properties of molecular weight (MW) and specific gravity
(SG) for the Cn+ fraction where n equals 7, 8, 9, or 10 based on the selection made
during Project Setup.
5. Click OK to exit the dialog.
Low Pressure Gas Input

If Low Pressure Gas is selected as the known separator stream in Project Setup, the Low
Pressure Gas Input dialog will appear when you click on the Separator hotspot.
To specify low pressure gas:

1. Click on the Separator hotspot on the Input Flowsheet. The Low Pressure Gas Input
dialog appears.
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Separator: Low Pressure Gas Input

2. Provide Separator Conditions: Pressure and Temperature.
3. Enter Compositional data for each component.
4. Provide the characterization properties of molecular weight (MW) and specific gravity
(SG) for the Cn+ fraction where n equals 7, 8, 9, or 10, based on the selection made
during Project Setup.
5. Select Molar GOR or Volumetric GOR:
If Molar GOR is selected, enter the value in the Molar GOR box.
If Volumetric GOR is selected, click Enter Volumetric GOR and then Enter GOR
dialog appears. Enter volumetric GOR, oil density and MW. Click Convert to Molar
GOR. You will return to the Low Pressure Gas Input dialog.
6. Click OK to exit the Low Pressure Gas Input dialog.
Note: If the separator pressure data are in units of psig, the user should convert to psia. Since
the local ambient pressure varies with elevation and meteorological conditions, the program
requires the user to enter pressure in absolute units.
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Geographical Database
If you do not have any stream data on the separator, you may select the Geographical
Database option in the Project Setup window. This option offers a selection of 103 cases that
are stored in a database sorted according to their geographical regions, sales oil, and separator
conditions. The parameters for each case are taken from actual field data. The separator oil
compositions are also associated with the selection of these cases. Hence, the separator
compositions are automatically fixed upon the selection of a geographical site and a specific
case.
To select a case from the database:

1. Click on the Separator hotspot on the Input Flowsheet. The Geographical Database
dialog appears.
Separator: Geographical Database

2. Select a region closest to the actual geographical location of your facility.
3. Select a case closest to the actual sales oil data and separator conditions.
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4. After the selections made in Step 2 and Step 3, the composition of the low-pressure oil is
automatically displayed in the left pane.
5. Click OK to accept selection and exit the dialog.
Stable Oil Tank

If you select the Stable Oil Tank flowsheet, the program will calculate only the working and
standing losses from the storage tank for stable oil.
Data Input Flowsheet: Stable Oil Tank
Stable Oil
This input is required if you select the Stable Oil Tank flowsheet. In order to execute the standalone AP-42 calculations, users must provide the compositions of the stable oil entering the
storage tank.
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To specify stable oil:

1. Click on the Stable Oil hotspot in the input flowsheet.
Stable Oil Input
2. Enter the stable oil Compositions.

3. Enter the Cn+ characterization properties.
4. Click OK to return to the Input Flowsheet.
Tank Information Input

If the AP-42 method is selected for W&S losses during project setup the Oil Tank is presented
as a hotspot in the Data Input window. Otherwise (RVP Distillation Column Method selected)
tank information is not required to estimate the losses and the oil tank is greyed out and
disabled as a hotspot.23.
To provide oil tank information:

1. Click on the Oil Tank hotspot to activate the Tank Information dialog. There are two
tabs in the dialog: Tank & Shell Info and Meteorological Info.
2. Click on the Tank & Shell Info. tab.
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Oil Tank: Tank & Shell Information
3. Provide the tank dimensions.

4. Enter normal working conditions such as Average Liquid Height and Breather Vent
Pressure Setting Range.
5. In the Solar Absorbance section, select a color from the Paint Color box. Click to
assign the paint condition. The program will adjust the paint factor accordingly.
Otherwise, simply enter the factor, if known, into the Paint Factor box directly.
6. Click on the Meteorological Info. tab.
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Oil Tank: Meteorological Information
7. Select a city closest to the geographical location of the facility.

8. Upon selecting a US location, the program automatically displays the Daily Minimum
and Maximum ambient temperatures as well as the Daily Solar Insolation. These
values may be edited to reflect actual location data, if available. Editing these values is
recommended where significant climate differences from the nearest geographical
location may exist because of elevation differences or other meteorological factors.
9. Enter the Ambient Pressure. This pressure value may have already been updated from
the Flash Valve Inputs dialog but may be adjusted here, if necessary.
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Note: The solar absorbance factors of paint are taken from an AP-42 publication [8] based on
the conditions of the tank.
Sales Oil
If the RVP Distillation Column method is selected, the sales oil properties required as inputs in
the Sales Oil dialog are production rate, days of annual operation, API gravity, and Reid vapor
pressure. If the AP-42 method is selected the bulk temperature of the sales oil is an additional
parameter required to be input. These data are commonly available. If the calculation is on the
monthly basis, the production rate and actual number of operating days in each month should
be entered.
To specify sales oil:

1. Click on the Sales Oil hotspot in the Data Input flowsheet.
Sales Oil Input
2. Enter the sales oil properties in the appropriate boxes.

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Flash Valve
To specify the flash valve inputs:
1. Click on the Flash Valve hotspot in the Data Input flowsheet.
Flash Valve Inputs
2. Enter the Ambient Pressure and Ambient Temperature. If the ambient temperature is
unavailable, use temperature of the upstream separator.
3. Click OK to return to the Input Flowsheet window.
Note: The flash valve is not a physical piece of equipment. It simply illustrates pressure
reduction in a flow line.
Air Injection
Air or gas injection is optional. It is introduced into the system as an air and/or gas blanket. This
option is available to RVP Distillation method only.
To specify an air injection:

1. In Project Setup, select the Air Injection box in the Configuration tab.
2. Proceed to the Data Input window.
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3. Click on the Air Injection hotspot on the Input Flowsheet. The Air/Gas Input dialog
appears.
Air Injection
4. Enter the daily air/gas injection volume.
5. Provide the air/gas Compositions.
Data Output
Predicted results are viewed in the Data Output window. The program will advance to the Data
Output window once the calculations have converged.
Viewing Calculation Results

The calculated results are presented in the Data Output window. The outputs are shown in four
tabs:
Output Flowsheet
Emission Summary
Emission Compositions
Stream Data
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If monthly calculations are selected, Total HAPs, Total HC, VOCs, and emissions of CO2 and
CH4 are tabulated for comparison on a monthly basis and monthly plots are available by clicking
on the chart icon on the toolbar.
Output Flowsheet
Clicking on a hotspot (colored red) in the Output Flowsheet activates a pop-up dialog that
consists of compositional information and stream properties for the selected hotspot.
Note: Output flowsheet is not available when running monthly calculations.
Output Flowsheet
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Emission Summary
This tab contains the controlled and uncontrolled emissions for components of specific interest.
They are the Total HAPs, Total HC, VOCs, C2+, VOCs, C3+, CO2, and CH4. Note that because
emissions of Greenhouse Gases (GHG), specifically CO2, will depend on the control strategy
(i.e. combustion vs. vapor recovery), controlled emissions of GHG are left to the user to
calculate on a facility-specific basis.
This tab also lists the uncontrolled recovery for Vapor, HC Vapor, CO2, CH4, and GOR from the
oil storage tank.
Emission Summary
Similar to the Emission Summary tab, this tab presents the controlled and uncontrolled
emissions for all the components in your system. In this list, control efficiency is applied to the
combustible components and the non-combustible components pass through unaltered by the
control efficiency factor. However, since control strategies vary combustion products are NOT
calculated by the program so that CO2 emissions must be calculated via other methods.
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Stream Data
This tab shows the compositions for all the different streams as well as their physical and
thermodynamic properties.
Stream Data
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Emission Summary Plot

When running monthly calculations, the emission results (controlled Total HAPs, Total HC,
VOCs, C2+, VOCs, C3+, and uncontrolled CO2 and CH4) based on the selected months are
plotted for comparison by selecting the chart icon on the toolbar.
Emission Plot
Printing Calculation Results

To print calculation results:
1. Select Print from the toolbar or from the File menu. The Print Report dialog appears.
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Selecting a Print Item

2. Select an item to print. Click OK. The E&P TANK Print Preview dialog appears.
Print Preview
3. Click Print to start printing. Alternatively, you can save the report to a file or copy the
report to another location or Export to excel.
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To copy results from Print Preview:

1. While you are in the E&P TANK Print Preview dialog, select contents to copy by
highlighting the selection.
2. Click Copy.
3. Proceed to the destined location or application and click Paste from within the
application.
To Export Results to Excel

1. Right-click the mouse (or use Ctrl+E shortcut) and select Send to MS Excel on the
toolbar. This will automatically export the current screen to Excel.
2. Select Print from the toolbar or from the File menu. The Print Report dialog appears.
Select an item to print. Click OK, then click Export to excel, it allows the user to export
current data or the whole project.
Print to MS Excel
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Copy and Paste

E&P TANK is equipped with a copy and paste feature that allows tedious compositional data
to be transferred from external spreadsheets such as Microsoft Excel worksheets.
To copy data from a Windows application

1. Select and copy cells in the external spreadsheets.
2. Start E&P TANK 3.0 and select destination cells in the E&P TANK Worksheet.
3. Select Paste from the Pop-up menu.
To copy data to a Windows application

1. Select data from an E&P TANK worksheet.
2. Right-click the mouse and select Copy and Copy ALL from the pop-up menu.
3. Go to the Windows application and select destination cells in the spreadsheet.
4. Perform the Paste command while in the Windows application.
Chapter 5: Managing Projects

E&P TANK Projects can be created, saved, printed in the text file format or from the Microsoft
Excel environment (for terminals with Microsoft Excel), and deleted.
To Create a New Project

When you are starting E&P TANK v3.0:
In the welcome window, select Create a New E&P TANK Project and click OK.
-orWhile you are working on another project:
Click on the New Project button on the toolbar or select New from the File menu.
To Open an Existing Project

1. When you are starting E&P TANK v3.0:
Select Open an existing E&P TANK project and click OK
-orWhile you are working on another project:
Click on the Open E&P TANK Project File button on the toolbar or select Open...
from the File menu.
The Open E&P TANK dialog appears.
2. Specify the file path and the file name.
3. Click Open.
To Print a Project
To print a project in text file format (if Microsoft Excel is not installed in your computer):
1. Click on the Print button on the toolbar or select Print... from the File menu.
2. In the Print Report dialog, select an item to print and click OK.
3. In the E&P TANK Print Preview dialog, click Print to start printing.
While you are in the E&P TANK Print Preview dialog, you can also save the calculation results
to a file for future review or copy the results into another location for editing.
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If Microsoft Excel is installed in your computer, refer to To Export Results to Excel to obtain
a hard copy of the project in the Excel format.
To Save a Project
Click on the Save button on the toolbar or select Save from the File menu.
To Save a Project into Another File Name

1. Select Save As... from the File menu. The Save E&P TANK Project File dialog
appears.
2. Specify the file path and file name.
3. Click Save.
Saving a Project
To Delete a Project
In Windows Explorer, select the project file click Delete.
Annex A: Technical Background

A simplified flow diagram of a typical oil production tank system is illustrated in Figure 1. The
liquid oil from a low pressure (LP) separator, after passing through a pressure reducing valve, is
charged into the production tank where it may be stored for a period of time before being
shipped as sales oil. The emission losses from the tank can be classified into three categories:
flash, working, and standing (also called breathing) losses. Flash losses occur when the
pressure of the saturated oil is reduced from some moderate pressure in the LP separator to
atmospheric pressure in the storage tank. For a typical production tank, the flash loss forms a
major contribution to its overall emissions. Working losses are vapors displaced from the tank
during the filling cycle, and standing losses are vapors generated through diurnal and seasonal
temperature changes.
Figure 1Oil Production Storage System
It is important to note the relationship between the LP separator and the flash calculation
performed at the entrance to the storage tank. Currently, the Oil Tank module completes the
flash calculation at a user specified ambient temperature. This temperature is necessary as it
will produce the most accurate representation of the losses at the flash valve. However, if this
ambient temperature is not available, the user can provide the previously recorded separator
temperature for the most conservative estimate of the flash losses.
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Following the inlet flash calculation are the tank operations. The operation of the fixed roof tank
is simulated by a distillation column with four trays operation. Similarly to the flash valve, the
produced vapor also contributes to the total tank emissions, while the liquid phase from the fixed
roof tank represents the sales oil.
Working and standing losses are highly dynamic in nature and cannot be described solely by
steady-state models. However, since most of the dynamic information, such as meteorological
and daily liquid level data, is cumbersome to use, an inference method was designed to
circumvent this difficulty [1]. The method imposes a constraint that the characteristics of the
liquid effluent from the storage tank should match the sales oil characteristics (e.g., RVP and
API gravity). This inference method ensures that all effects of dynamic parameters are suitably
represented by the simulator. The shortcoming of using this inference method is that the model
may artificially adjust some operating parameters of the tank to reflect the effects of dynamic
parameters. For example, the model may be forced to raise the operating temperature of the
storage tank beyond that actually encountered to compensate for the elevated emission level
resulting from extended residence times of the sales oil.
In E&P TANK, two different alternatives for estimating flashing, working, and standing losses
are provided. The first alternative estimates the flash loss using rigorous thermodynamic flash
calculations and estimates working and standing losses with a fixed roof tank simulation. Here,
a four-tray distillation column representation is attempted. In this case, detailed information such
as tank characteristics and site meteorological data are not necessary to estimate emissions.
The minimum information requirements for this method are:
Separator Pressure and Temperature
Separator Oil Composition
Reference Pressure
RVP of Sales Oil
Sales Oil Production Rate
API Gravity of Sales Oil
The second alternative estimates the flash losses using the same rigorous thermodynamic flash
calculations as in the first method. However, working and standing losses are estimated using
the modified AP-42 equations which require details on tank characteristics and site
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meteorological data. In addition to the information requirements listed above for the first
approach, at a minimum, the second approach requires the following input data:
Stock Oil Bulk Temperature
Tank Diameter
Tank Shell Height
Average Stock Liquid Height
Cone Roof Slope
Tank Solar Absorbency
Daily Minimum Ambient Temperature
Daily Maximum Ambient Temperature
Daily Solar Insulation
Breather Vent Pressure Setting Range
Both approaches are available to the user, thereby allowing emission estimates to be made
depending upon data availability and user needs. In general, the first approach will yield more
conservative (i.e. higher) emission estimates than the second approach.
Influent Specifications
There are several modes for users to specify influent data for the model (i.e. the model is able to
accept different types of compositional input data). Each of the options that follow either accepts
or completes a calculation to generate the LP separator oil composition. It is this fluid that
undergoes flashing, working and standing losses to produce emissions.
Input Option 1: LP Separator Oil

The first input option is to directly specify the LP separator oil composition of the liquid
discharged from the final LP separator. This is the preferred option and a sampling protocol is
given in Annex C to ensure proper oil sample collection. This is a commonly available analysis
and provides the simplest operation of the model.
Input Option 2: HP Separator Oil

A second option is to enter the composition of a high pressure fluid stream and allows the model
to complete a flash calculation through the low pressure separator.
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Input Option 3: LP Separator Gas

The third option is to enter the composition of a separator gas sample with a measured Gas-Oil
Ratio (GOR). With these data, the software will complete a recombination calculation to
determine the composition of the LP separator oil.
Input Option 4: Geographical Database

Finally, it is possible to obtain compositional input data from the Database option. This database
contains 103 example cases (containing both fluid compositions and tank operating conditions)
obtained from API. These cases are taken from actual tank sites across the US. These example
cases may be selected by geographical location or by oil physical properties. The geographical
criteria are useful in providing conditions based on location while the oil selection capability aids
in the comparison of emission losses from oils with different physical characteristics. It is also
important to note that these example cases may be manipulated and adjusted based on any
measured data that are available.
In terms of compositional data requirements, the model has been designed to accept C7+, C8+,
C9+, C10+ analyses with a detailed breakdown of the HAP and VOC components. A flexible
plus fraction characterization has been implemented. The characterization is performed by
employing an exponential distribution function and a process of critical properties estimate for
pseudo-components to represent the fractions with carbon number greater than 7. The
characterization procedure from the literature [2] is adapted and it involves the following steps:
1. Generate molecular weight and density for each component using exponential
extrapolation.
2. Generate critical properties and interaction parameters for each component using the
property correlation.
3. Group or lump components and generate pseudo-components properties that are
required in the EOS calculations.
The corresponding C7+, C8, C9+, C10+ molecular weight and specific gravity are required to
characterize the pseudo-component in the model. The case studies show that the predicted
emission results after implementing the new charateriztion algorithm are an improvement over
the previous version predictions.
39
Modified AP-42 for Non-Flash Tank Emissions

The AP-42 method has been generally accepted for estimating working and standing (nonflashing) losses for stabilized hydrocarbon products with an RVP of 12 psia or less. The AP-42
method cannot distinguish between HAPs and VOCs for crude oil. The E&P TANK modifications
have remedied this shortcoming.
The documented AP-42 method [3] uses empirical correlations for estimating evaporative (nonflash) losses from fixed-roof tanks. The data required to use the AP-42 method can be classified
into three categories:
1. Tank Characteristics
2. Meteorological Information
3. Oil Specifications
Tank characteristics include tank shape and size, paint color, average liquid height, and
breather vent pressure setting. Meteorological information includes daily maximum and
minimum ambient temperature, solar insolation on a horizontal surface, and reference ambient
pressure. Oil specifications include oil RVP and throughput. Separate empirical correlations are
applied for both working and standing losses in a specified time period and results are
presented in units of emission (for example, ton or lb).
The modification of the AP-42 method in this package is focused on oil specifications. Rigorous
thermodynamic calculations based on the Peng-Robinson EOS [4] have been introduced to
characterize oils whenever necessary. A summary of changes is provided as follows:
Oil RVP is calculated by the Peng-Robinson EOS according to the composition

specifications.
The AP-42 method is deemed unsuitable if the oil vapor pressure at the specified
average tank temperature equals or exceeds the reference ambient pressure.
The evaporated oil composition is calculated from a hypothetical flash at 90 percent of

the saturation pressure.
Technical Basis of E&P TANK

E&P TANK is built upon rigorous thermodynamic calculations. All components and phases are
assumed to be in equilibrium throughout the entire system. For most hydrocarbon processes,
40
this assumption is a fairly good approximation. Also, the Peng-Robinson EOS [4] has been
chosen for property-related calculations because it is one of the most widely accepted models in
the hydrocarbon processing industry.
When vapor and liquid phases are in equilibrium, the fugacity of each component in the vapor
(fiV) is equal to its fugacity in the liquid (fiL). The fugacities in the liquid and vapor are defined by:
fi L iL xi P
f iV Vi yi P
where
P
is the system pressure,
xi
is the mole fraction of species i in liquid,
yi
is the mole fraction of species i in vapor,
iL
is the fugacity coefficient of species i in liquid,
Vi
is the fugacity coefficient of species i in vapor.
One advantage of using an EOS model is that the fugacity coefficients in both the vapor and
liquid phases are treated uniformly by the following relation:
ln i
1 P RT
PV

dV ln
RT V ni V
RT
where
is the either V for vapor or L for liquid phase
is the system pressure
is the system volume at the specified condition
is the system temperature on an absolute scale
is the universal gas constant
is the number of moles of species i.
The above thermodynamic relationships, in conjunction with material and energy balances, are
used extensively in the program to solve for vapor-liquid-equilibrium (VLE) conditions. Detailed
41
discussions about the calculation schemes for convergence are covered in standard
thermodynamic textbooks such as the one by Smith and Van Ness [5].
In particular cases where the VLE separation is achieved through column distillations, the
simulation of the column is accomplished using the Ishii-Otto [6] algorithm. The Ishii-Otto
algorithm is fairly stable and fast in reaching convergent solutions for most hydrocarbon
applications.
Annex B: Technical References

[1]
Choi, M., API Tank Vapors Project, Paper (SPE 26588) presented at the meeting of
68th Annual Technical Conference and Exhibition of the Society of Petroleum
Engineers. Houston, Texas: October 3-6, 1993.
[2]
Pedersen, K.S., Thomassen P. and Fredenslund Aa., paper presented at the AICHE
Spring National Meeting New Orleans LA, 6-10 March, 1988.
[3]
Gas Research Institute, Technical Reference Manual for GRI-GlyCalc: A Program for
Estimating Emissions from Glycol Dehydration of Natural Gas, Prepared by Radian
International LLC, 1996.
[4]
Peng, D.Y. and Robinson, D.B., A New Two-Constant Equation of State, Industrial and
Engineering Chemistry Fundamentals, 15(1):59-64, 1976.
[5]
Smith,
J.M.
and
Van
Ness,
H.C.,
Introduction
to
Chemical
Engineering
Thermodynamics, 3rd Edition, McGraw-Hill, New York, NY, 1975.

[6]
Ishii, Y. and Otto, F.D., A General Algorithm for Multistage Multicomponent Separation
Calculations, Canadian Journal of Chemical Engineering. 51: 601-606, 1973.
[7]
Radian International LLC, Evaluation of a Petroleum Production Tank Emission Model,

API Publication No. 4662 American Petroleum Institute, Washington, D.C., 1997
[8]
US Environmental Protection Agency, Compilation of Air Pollutant Emission Factors.

Vol. 1, Stationary Point and Area Emission Units, Section 7, AP-42, Fifth Edition
(January 1996); Supplements A and B (November 1996). Report prepared by Office of
Air Quality Planning and Standards, US Environmental Protection Agency, Research
Triangle Park, NC. 1996.
42
Annex C: Sampling Protocol

Surface Fluid Sampling of Black Oil Reservoirs
Separator Liquid Collection
The separator liquid sample collection point should be upstream of any metering device or flow
restriction to ensure single phase flow. There is often a temperature reduction on the separator
liquid flowline, but this does not alter the sample integrity. Conversely, if the flowline
temperature is in excess of the operating temperature of the separator, it is advisable to sample
directly from the sight gauge on the separator.
Care must be taken when sampling from the separator sight gauge. The upper and lower
values installed on sight gauges have restricted flow orifices and check valves. Therefore, as
fluids are removed through sight gauge valves, there is a preferred flow of the gas phase
through the top valve. One must maintain the liquid level above the bottom sight glass valve
while collecting the separator liquid samples. If the liquid level is allowed to decrease to the
point of sample collection, excess gas will be drawn into the cylinder with the separator liquid,
voiding the validity of the separator liquid sample.
Flexible lines used to connect the sample source to the sample cylinder should be as short as
possible. One should check for entrained water in the liquid source stream.
Water and any other contaminant must be removed completely prior to the collection of any
separator liquid samples. It is advisable to re-check the sampling points and line for
contaminants after completing the sampling procedure to ensure proper samples have been
collected.
Separator Liquid Collection: Evacuated Cylinder Method

1. The cylinders should be evacuated by the laboratory before being sent to the field.
2. Select a sample point from which a representative first stage separator liquid sample can
be collected.
3. Compare the pressure and temperature of the sample source to the maximum operating
pressure and the current temperature of the sample cylinder to ensure that the cylinder
will safely contain the liquid sample. The cylinder temperature should not be more than
43
44
10 F (6 C) lower than the source temperature. If it is, this technique should not be
used. Low cylinder temperatures often cause the cylinder to fill completely with liquid,
thus resulting in a serious hazardous situation when the cylinder is allowed to warm. To
prevent the hazardous situation, an alternate technique, such as the Liquid
Displacement Method, should be used. The cylinder must be an approved type with a
current certification date for sample transport to the laboratory. In the United States, the
cylinder must be an approved type with a current certification date for sample
transportation to the laboratory. In the United States, the cylinder must be approved by
the U.S. Department of Transportation, while transporting a cylinder in many
international locations requires certification by Lloyds Register Industrial Services.
4. Connect the sampling line to the liquid source and the sample cylinder in the manner
shown in Figure C-1, leaving the fitting on the cylinder end of the connector line finger
tight.
Figure C-1. Evacuated Cylinder Method
5. Slowly purge the sample line to displace air and to vent sufficient liquid to clean the
sample point and sampling system.
6. With a wrench, properly tighten the connecting line fitting to the cylinder fitting.
7. With the sample line purged and full of liquid and the separator liquid source valve fully
open, hold cylinder in a vertical position with the inlet valve at the bottom and slowly (but
fully) open the lower cylinder valve to admit liquid into the container. Refer to Figure C-1.
45
8. When the liquid stops flowing into the cylinder, close the inlet valve before moving the
cylinder out of the vertical position. The sample collected in this manner will be in two
phases, gas and liquid. The sample cylinder will have some portion of its volume as gas
cap, which can safely accommodate any liquid expansion if the cylinder temperature
increases during shipment to the laboratory.
9. Close the valves from the sample source and de-pressurize the connect line. Dismantle
the sampling assembly and install the blow plug in the sample cylinder valve used for
sample entry.
10. Fill in information on the sample tag as completely and accurately as possible and attach
the tag to the sample cylinder. Also on a separate sheet of paper, make a list of all of the
information recorded on the cylinder tag along with the cylinder number. Prepare the
information for all cylinders involved in the sample collection on the sheet of paper for
separate mailing to the laboratory.
11. Repeat the above procedures using all separator liquid cylinders provided.
Notes (Item 8):
The (safe) situation of having a two phase system in the container will not change to an unsafe
single liquid phase situation unless one or more of the following is allowed to occur:
Sample container is agitated while filling.
Containers being filled are much colder than the separator.
Containers are left on the pressure source for an extended length of time. It is not
important to have the container completely full of sample. The representative liquid has been
admitted to the cylinder and is not altered in composition; it merely has been flashed to a two
phase condition for transport to the laboratory. When this sample is received in the laboratory, it
is pressured up to considerably above the source pressure by mercury injection prior to removal
of any portion of the contents. During the re-pressurization, the saturation pressure is measured
to check the validity of the sample contained. If the saturation pressure obtained does not
approximate the separator conditions, any subsequent analysis performed using the sample will
be in error.
Medium gravity, 20 to 27 API crude oils are particularly susceptible to foaming and, if sampled
directly into an evacuated cylinder, could result in obtaining a cylinder virtually full of gas with a
small amount of foamy oil. The procedure of sampling a liquid by gas displacement is used to
overcome this potential foaming problem. The description of this procedure begins below.
46
Separator Liquid Collection: Gas Displacement Method

1. Select a sample point from which a representative first stage separator liquid sample can
be collected.
2. Compare the pressure of the sample source to the maximum operating pressure of the
sample cylinder to ensure that the cylinder safely contains the liquid sample. The
cylinder must be an approved type with a current certification date for sample transport
to the laboratory. In the United States, the cylinder must be approved by the U.S.
Department of Transportation, while transporting a cylinder in many international
locations requires certification by Lloyds Register Industrial Services.
3. Fill the cylinder to be used for collecting separator liquid sample with equilibrium
separator gas as per the procedure outlined in Separator Gas Collection - Evacuated
Cylinder Method.
4. Connect the sampling line to the liquid sample source and to the gas filled liquid sample
cylinder in the conventional manner shown in Figure C-1 leaving the fitting on the
cylinder end of the connecting line finger tight.
5. Slowly purge the sample line to displace air and to vent enough liquid to clean the
sample point and sampling system.
6. With a wrench, properly tighten the connecting line fitting to the cylinder fitting.
7. With the sample line purged and full of liquid and the sample source valve fully opened,
hold the cylinder in a vertical position as indicated in Figure C-1, with inlet valve at the
bottom and fully open the lower cylinder valve.
8. Holding the cylinder vertical, slowly open the top valve of the cylinder to bleed gas at a
very low rate. The low bleeding rate is necessary so no appreciable pressure drop
occurs in the sampling system, thus maintaining the separator liquid in one phase while
it enters the sample cylinder.
9. When separator liquid flows from the top valve, close first the top valve and second the
bottom valve of the cylinder. Close the valve from the source and depressurize the
sampling system.
10. Disconnect the sample cylinder from the sampling hose.
11. Holding the cylinder vertical, in a single motion quickly release a small amount of liquid
from the bottom valve. This will relieve the dangerous situation of having a cylinder
completely filled with liquid for transport to the laboratory, without altering the sample.
Creating a gas cap in this manner can easily alter the sample composition. In order to
47
prevent the alteration of the sample composition, the liquid must be taken in one quick
motion.
12. Install blow plugs securely in both valves.
13. Fill in information on the sample tag as completely and accurately as possible and attach
to the sample cylinder.
14. On a separate sheet of paper, list the cylinder number with all of the information
recorded on the sample cylinder tag. Include this information for all cylinders involved in
the sample collection on this same sheet of paper. Send this information under separate
cover to the laboratory.
15. Repeat the above procedure using all separator liquid cylinders provided.
Notes:
Medium gravity, 20 to 27 API, crude oils are particularly susceptible to foaming and if sampled
directly into an evacuated cylinder, could result in obtaining a cylinder virtually full of gas with a
small amount of foamy oil. The procedure of sampling a liquid by gas or liquid displacement is
used to overcome this potential foaming problem.
Separator Liquid Collection: Liquid Displacement Method

1. Fill the cylinder with a suitable liquid which is more dense than, and immiscible with the
separator liquid. Suitable liquids for use are displacement media which are: mercury,
brine, glycol/water mixtures and water. The latter three should not be used in sour
systems.
2. Select a sample point from which a representative first stage separator sample can be
collected.
3. Compare the pressure of the sample source to the maximum operating pressure of the
sample cylinder to ensure that the cylinder will safely contain the liquid sample. The
cylinder must be an approved type with a current certification date for sample transport
to the laboratory. In the United States, the cylinder must be approved by the U.S.
Department of Transportation, while transporting a cylinder in many international
locations requires certification by Lloyds Register Industrial Services.
4. Connect the sample line to the separator liquid source and to the sample cylinder in a
manner as shown in Figure C-2, leaving the fitting on the cylinder end of the connector
line finger tight.
48
Figure C-2. Liquid Displacement Method
5. Partially open the separator liquid source valve, allowing a slow displacement of air from
the connecting line. Continue venting sufficient liquid to clean the sample point and
sampling system.
6. With a wrench, properly tighten the connecting line to the cylinder fitting.
7. Fully open the separator liquid source valve.
8. Maintain the cylinder in a vertical position with the inlet valve at the top throughout the
sample collection procedure.
9. Fully open the upper cylinder valve.
10. With the cylinder perfectly vertical, slowly open the bottom valve of the cylinder to allow
a slow (small) stream of displacement liquid to drain into a graduated cup.
11. Maintain the slow rate of displacement liquid removal so that no appreciable pressure
drop occurs in the sampling system. One must not rush this procedure.
12. When 90 percent of the sample cylinder volume has been collected, close first the
bottom valve and then the top valve of the sample cylinder.
13. With the top valve of the cylinder closed, slowly drain from the bottom of cylinder the
remaining 10 percent of the displacement liquid. Close the bottom valve of the sample
cylinder immediately when the separator liquid appears. Creating a gas cap in this
manner is easily accomplished, perfectly safe and of very little risk to the integrity of the
sample.
49
14. Close the valve from sample source and depressurize the sampling system.
15. Disconnect the sample cylinder from the sampling hose.
16. Securely install blow plugs into both sample cylinder valves.
17. Fill in information on the sample tags as completely and accurately as possible and
attach to the sample cylinder.
18. On a separate sheet of paper, list the cylinder number with all of the information
recorded on the sample cylinder tag. Include this information for all cylinders involved in
the sample collection on this same sheet of paper. Send this information under separate
cover to the laboratory.
19. Repeat the above procedure using all separator liquid cylinders provided.
Notes:
The Liquid Displacement sampling technique is generally utilized when collecting LPG and NGL
samples. This procedure ensures a good gas cap inside the cylinder. Samples of these
products can be extremely dangerous if the cylinder is absolutely liquid filled and allowed to
warm while in transport to the laboratory.
Separator Gas Collection

The gas sampling method is important for accurate modeling results. The separator gas sample
is typically collected from the gas line at the low pressure separator outlet. Operators have
sampled separator gas for years by attaching a canister or high pressure cylinder directly to the
separators gas sampling port. The GRI-GlyCalc manual (GRI, 1996) recommends employing a
manifold to remove entranced liquids from the sample probe when collecting the sample from
the gas line. The manifold is necessary when measuring low concentration components such as
HAPs (benzene, toluene, ethyl-benzene, xylenes and x-hexane). The manual recommends the
Gas Processors Association (GPA) standard 2166 as a gas sampling reference. Also, the
manual indicates a modified EPA method T0-14, normally used for ambient air sampling, as a
satisfactory method for gas sampling.
Index
Output ................................................. 24, 25
Paste ......................................................... 32
Printing Results ......................................... 29
Project Setup ............................................ 12
Projects ......................................... 12, 33, 34
creating ............................................ 12, 33
deleting .................................................. 34
opening .................................................. 33
Printing a Project ................................... 33
saving .................................................... 34
References ................................................ 42
Sales Oil .................................................... 22
Saving ...................................................... .34
a project ................................................. 34
Stable Oil .................................................. 18
System Requirements ................................ 6
Technical ............................................. 39, 42
Technical Basis ..................................... 39
Technical References ........................... 42
Welcome ..................................................... 1
Adding ................................................. 12, 33

Air Injection.......................................... 23, 24
Application Window ..................................... 8
Basic Steps ................................................. 8
Copy .......................................................... 32
Creating ............................................... 12, 33
a new project ................................... 12, 33
Deleting
a project ................................................. 34
Flash Valve................................................ 23
Geographical Inputs .................................. 17
Hardware Requirements ............................. 6
High Pressure Oil ...................................... 14
Key features ................................................ 1
Low Pressure Gas ..................................... 15
Low Pressure Oil ....................................... 14
LP/HP Oil Inputs ........................................ 15
Main window ............................................... 8
Navigating ................................................... 8
Oil Tank ..................................................... 19
50

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Production Tank Emissions Model,

E&P TANK Version 3.0

API PUBLICATION 4697

Whats New in This Version

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

3. Mass Balance and Green House Gas Emission Calculations

A choice of either monthly or yearly report display options.

API PUBLICATION 4697

The ability to export input / output results to MS Excel spreadsheet.

6. Compatibility between Version 2.0 and Version 3.0

About E&P TANK Version 3.0

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

Chapter 2: Installation and Security Methods

70 MB free hard disk space

Microsoft Windows 7/XP/2000/Vista

Microsoft Excel (for option to export)

Microsoft Network TCP/IP

Installing E&P TANK v3.0

Chapter 3: Getting Started

An introductory screen followed by the welcome window appears.

Welcome to the E&P TANK Program

API PUBLICATION 4697

To Exit E&P TANK v3.0

Click Exit from the File menu.

Click on the Close Box on the E&P TANK title bar.

Basic Steps to Generate an E&P TANK Project

Select a flowsheet and a calculation model

Specify necessary setup information

Provide the project information if available

Data Operating Area

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

Data Operating Area

The E&P TANK Application Window

API PUBLICATION 4697

Default Unit System Selection

Default Unit System Selection

Conversion Parameters Tab

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

To perform unit conversions:

Input the Value to be converted in the white blank area.

Chapter 4: Using E&P TANK Version 3.0

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

Stable Oil Tank

Stable Oil and Sales Oil

Flash Valve Inputs

API PUBLICATION 4697

Input Flowsheet: Tank with Separator

Data Input for Low Pressure or High Pressure Oil

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

To input data for the LP/HP Oils:

Separator: High Pressure Oil Input

2. Provide Separator Conditions: Pressure and Temperature.

Low Pressure Gas Input

To specify low pressure gas:

API PUBLICATION 4697

Separator: Low Pressure Gas Input

PRODUCTION TANK EMISSIONS MODEL, E&P TANK VERSION 3.0USERS MANUAL

To select a case from the database:

Separator: Geographical Database

API PUBLICATION 4697

Stable Oil Tank

Data Input Flowsheet: Stable Oil Tank